scholarly journals SYNTHESIS AND CHARACTERIZATION OF Cu (II) COMPLEXS WITH 1,4,8-TRIS(2-HIDROXYMETHIL)-11-METHYL-1,4,8,11-TETRAAZACYCLOTETRADECANE

2010 ◽  
Vol 3 (2) ◽  
pp. 70-73 ◽  
Author(s):  
Sentot Budi Rahardjo

Cu (II) complexs with 1,4,8-tris(2-hidroxymethyl)-11-methyl-1,4,8,11-tetraazacyclotetradecane (L) have been synthesized with chemical formula of [CuL](ClO4) (experimental Cu = 32.7 %, H = 6.4%, theoritical Cu = 32.6 %, H = 6.4 %). Its magnetic moment of 1.90 BM indicated that the complexs is paramagnetic and there are no Cu-Cu bonding. This complexs is stable with the value of log k [CuL]2+ = 17.3(2). Visible spectra of [CuL]2+ showed that single wide peak at λmax of 628 nm (ε = 164 dm3.mol-1.cm-1) and indicated of E9 - T29 transition. The IR spectra and the conductancy data indicated that the ClO4 was not coordinated to Cu.   Keywords: tembaga (II), senyawa kompleks, paramagnetik

2016 ◽  
Vol 13 (2) ◽  
pp. 244-252
Author(s):  
Baghdad Science Journal

In this paper, some chalcone derivatives (C1, C2) were synthesized based on the reaction of equal amount of substituted acetophenone and substituted banzaldehyde in basic medium. Oxazine and thiazine derivatives were prepared from the reaction of chalcones (C1-C2) with urea and thiourea respectively in a basic medium. Pyrazole derivatives were prepared based on the reaction of chalcones with hydrazine mono hydrate or phenyl hydrazine in the presence of glacial acetic acid as a catalyst. The new synthesized compounds were identified using various physical techniques like1 H-NMR and FT-IR spectra.


Author(s):  
Anca EMANDI

A new series of oxovanadium(IV) chelates containing bi-and tridentate pyrazol-5-one azo derivatives ligands of the type (I) [VO(L)2] and (2) [VO(L)(H2O)] have been prepared and characterized by elementary analysis, IR, electronic spectra, conductance measurements, and molecular weights. The ligands coordinate through (O-N) donor system as monobasic and bidentate (HL) for the first type and through (0-N-O) donor system as dibasic and tridentate (H2L) for the second type of complexes. The molecular weights, the presence of the (V=O) stretching band around 950 cm -1, and the visible spectra suggest a monomeric penta-coordinated structure for these complexes.


2013 ◽  
Vol 10 (3) ◽  
pp. 597-606
Author(s):  
Baghdad Science Journal

New (pentulose-?-lactone-2,3-enedibenzoate barbituric acid) (L) have been synthesized by reaction of (5-C-dimethyl malonyl-pentulose-?-lactone-2,3-enedibenzoate) with urea in alkaline media (sodium methoxide). (Ca+2, Co+2, Ni+2, Cu+2, Zn+2, Cd+2 and Hg+2) complexes of (pentulose-?-lactone-2,3-enedibenzoate barbituric acid) (L) have been prepared and characterized by (1H and 13CNMR), FTIR, (U.V-Vis) spectroscopy, Atomic absorption spectrophotometer (A.A.S), Molar conductivity measurements and Magnetic moment measurements, and the following general formula has been given for the prepared complexes [MLCl2(H2O)].XH2O, where M = (Ca+2, Co+2, Ni+2, Cu+2, Zn+2, Cd+2, Hg+2), X = five molecules with (Cd+2) complex, L = (pentulose-?-lactone-2,3-enedibenzoate barbituric acid).


2004 ◽  
Vol 59 (5) ◽  
pp. 554-558 ◽  
Author(s):  
Amar Srivastava ◽  
A.K. Shrimal ◽  
Amar Nath

Abstract Reactions of five sym-diarylthioureas (L), viz,, sym-diphenylthiourea (dptu), sym-di-o-tolylthiourea (dottu), sym-di-p-tolylthiourea (dpttu), sym-di-o-anisylthiourea (doatu) and sym-di-α- naphthylthiourea (dαntu) with W(CO)6 have been performed both by reflux and ultra-violet irradiation methods in which only monosubstituted products [(L)W(CO)5] are obtained. Several mixed ligand tungsten carbonyl derivatives, viz., [(o-phen or 2,2’-bipy)(L)W(CO)3] and [(Ph3P or Ph3As)(L)W(CO)4] have also been synthesized. Halogenation of [(L)W(CO)5] yielded heptacoordinated [(L)W(CO)4X2] (X = Br or I). The complexes have been characterized by microanalytical data, conductivity and IR measurements. The C-O stretching force constants and CO-CO stretch-stretch interaction constants of [(L)W(CO)5] derivatives have also been evaluated from the IR spectra.


2013 ◽  
Vol 17 (06n07) ◽  
pp. 573-586 ◽  
Author(s):  
Çiğdem Yağcı ◽  
Ahmet Bilgin

A phthalonitrile precursor 4-(3-hydroxypropylmercapto)phthalonitrile (3) was synthesized via a base-catalyzed nucleophilic aromatic nitro displacement of 4-nitrophthalonitrile with the 3-mercapto-1-propanol. A novel tetrasubstituted metal-free phthalocyanine (4) ( M = 2 H ) and its metal complexes (5–8) ( M = Zn , Ni , Cu and Co ) bearing 3-hydroxypropylmercapto moieties were prepared by the cyclotetramerization reaction of (3) with the appropriate materials. The visible spectra of the zinc(II) phthalocyanine (5) was recorded with different concentrations and different ions as Ag +, Hg 2+ and Pb 2+ in DMF and also with different solvents as dimethylformamide and pyridine. Fluorescence spectrum of the compound (5) was also studied. Temperature and frequency dependence of AC conductivity for (4–8) was investigated in air and under vacuum and were found to be ~10-8–10-5 S.m-1. Thermal properties of the phthalocyanines were examined by differential scanning calorimetry. All the novel compounds have been characterized by elemental analysis, UV-vis, FT-IR, NMR and MS spectral data and DSC techniques.


1975 ◽  
Vol 53 (17) ◽  
pp. 2657-2663 ◽  
Author(s):  
Mohamed A. S. Goher

The preparation of Cu(I) complexes of methyl isonicotinate, MeIN, of the formula (MeIN)nCuX, in which n = 1,2, 3, and 4 and X is Cl, Br, I, CN, SCN, and ClO4, has been described. The isolated complexes are characterized by their analytical data, diamagnetism, and conductivity measurements. The M → L charge transfer bands in the visible spectra and the i.r. spectra of these complexes are discussed.


2022 ◽  
Vol 890 ◽  
pp. 161825
Author(s):  
Harikrishnan Ravichandran ◽  
Baskaran Irusan ◽  
Sathyaseelan Balaraman ◽  
Mani Govindasamy ◽  
Senthilnathan Krishnamoorthy ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
H. D. Juneja ◽  
Manisha Joshi ◽  
J. P. Kanfade

The oxaloyl carboxymethyl cellulose (OCMC) complexes of Mn(II), Co(II), Ni(II), Cu(II), and Zn(II) metal ions have been synthesized and the coordination of OCMC in these complexes has been investigated through IR spectra, reflectance spectra, and thermal analysis. On the basis of spectral and thermal data an octahedral geometry was assigned to[Mn(II)OCMC(H2O)2]nand[Co(II)OCMC(H2O)2]n, square planar geometry was assigned to[Cu(II)OCMC]n, and tetrahedral geometry was assigned to[Ni(II)OCMC]nand[Zn(II)OCMC]nMetallic Gel complexes.


2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
A. K. Yadava ◽  
H. S. Yadav ◽  
Sanjay Singh ◽  
U. S. Yadav ◽  
D. P. Rao

A series of oxovanadium(IV) complexes of the type [VO(mac)]SO4(where mac = tetraazamacrocyclic ligands derived from condensation of 4,4,4-trifluro-1-(2-furyl)-1,3-butanedione or 4,4,4-trifluro-1-(2-thenyl)-1,3-butanedione withp-phenylenediamine and their reaction withβ-diketones) have been prepared using oxometal ion of vanadium as kinetic template. These complexes have been ascertained by electrical conductance, magnetic moment, elemental analyses, infrared, e.s.r. and electronic spectral data. All the oxovanadium(IV) complexes are five-coordinate ones.


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